- Parexel (Sacramento, CA)
- …investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical ... /scientific writing skills. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or… more
- Pfizer (South San Francisco, CA)
- …development program meets scientific, ethical, and regulatory standards. **Job Responsibilities** Clinical Development Leadership on Study Teams and Development ... investigators + Serve as the point of contact for clinical issues between the study team, investigators,...of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory… more
- University of Southern California (Los Angeles, CA)
- …Southern California Institute for Addiction Science is seeking an experienced clinical research coordinator to fill a full-time Research Coordinator Supervisor ... candidate will play a central role in the management of single-site and multi-site clinical trials to evaluate new treatments for addiction, with a primary focus on… more
- Genentech (South San Francisco, CA)
- …embedding patient-centered and AI-enabled digital solutions into the fabric of clinical research. By integrating data science, measurement science, and digital ... and regulatory-ready innovations that enhance trial design, evidence generation, and clinical value of Roche medicines. **The Opportunity:** As the Therapeutic Area… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …data, including registries, claims, and electronic health records, to support RWE studies . The Director manages a team of epidemiologists and data analysts engaged ... in RWE studies . The role also entails collaboration with the cross-functional...role also entails collaboration with the cross-functional team including Clinical , Medical, Safety, Commercial, Research, and Technical Operations, to… more
- Cedars-Sinai (Los Angeles, CA)
- …process and will review and remain current on literature as it relates to clinical /research study . This position coordinates all lab and/or clinical ... grant funds. **Primary Duties and Responsibilities:** + Provides miscellaneous clinical /research support (ad hoc data analysis, hypothesis development, programming,… more
- Parexel (Sacramento, CA)
- …Partner is a crucial liaison for investigative sites throughout a study 's lifecycle, responsible for site start-up, activation, relationship management, recruitment, ... + Maintains a knowledge of assigned protocols + Conducts study start-up activities at the site level including but...for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness… more
- Pfizer (South San Francisco, CA)
- …enrich the SCP (based on wide cross-functional input) with evolving evidence from clinical studies , insights, the Clinical Development Plan and regulatory ... + Chair Scientific Publications Committees (SPCs) + Work closely with clinical study teams during data readouts to determine publication content + Ensure… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …sustained development efforts and managing projects + Experience in and/or managing studies including literature reviews, study development and execution, and ... Risk-Benefit determinations, the development of post market risk estimation criteria, Clinical Evaluation Reports, and support of internal / external audits. **Job… more
- Gilead Sciences, Inc. (Foster City, CA)
- …approaches to optimize study parameters and interpret outcomes. + Prepare study protocols and coordinate execution of nonclinical studies which may involve ... responsibilities include designing and interpreting in vitro and in vivo studies , integrating data into mathematical models, and generating simulations to support… more